Heterologous Prime/Boost Immunization of Rhesus Monkeys by Using Diverse Poxvirus Vectors
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Published in | Journal of Virology Vol. 81; no. 16; pp. 8563 - 8570 |
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AbstractList | ABSTRACT
As the diversity of potential immunogens increases within certain classes of vectors, the possibility has arisen of employing heterologous prime/boost immunizations using diverse members of the same family of vectors. The present study was initiated to explore the use of divergent pox vectors in a prime/boost regimen to elicit high-frequency cellular immune responses to human immunodeficiency virus type 1 envelope and simian immunodeficiency virus
gag
in rhesus monkeys. We demonstrated that monkeys vaccinated with a recombinant modified vaccinia virus Ankara (rMVA) prime/recombinant fowlpox virus (rFPV) boost regimen and monkeys vaccinated with a recombinant vaccinia virus prime/rFPV boost regimen developed comparable cellular immune responses that were greater in magnitude than those elicited by a homologous prime/boost with rMVA. Nevertheless, comparable magnitude recall cellular immune responses were observed in monkeys vaccinated with heterologous and homologous recombinant poxvirus following challenge with the CXCR4-tropic SHIV-89.6P. Consistent with this finding, comparable levels of containment of viral replication and CD4
+
T-lymphocyte preservation were seen in these groups of recombinant poxvirus-vaccinated monkeys. This study supports further exploration of combining recombinant vectors of the same family in prime/boost immunization strategies to optimize vaccine-elicited cellular immune responses. Article Usage Stats Services JVI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit StumbleUpon Twitter current issue Spotlights in the Current Issue JVI About JVI Subscribers Authors Reviewers Advertisers Inquiries from the Press Permissions & Commercial Reprints ASM Journals Public Access Policy JVI RSS Feeds 1752 N Street N.W. • Washington DC 20036 202.737.3600 • 202.942.9355 fax • journals@asmusa.org Print ISSN: 0022-538X Online ISSN: 1098-5514 Copyright © 2014 by the American Society for Microbiology. For an alternate route to JVI .asm.org, visit: JVI As the diversity of potential immunogens increases within certain classes of vectors, the possibility has arisen of employing heterologous prime/boost immunizations using diverse members of the same family of vectors. The present study was initiated to explore the use of divergent pox vectors in a prime/boost regimen to elicit high-frequency cellular immune responses to human immunodeficiency virus type 1 envelope and simian immunodeficiency virus gag in rhesus monkeys. We demonstrated that monkeys vaccinated with a recombinant modified vaccinia virus Ankara (rMVA) prime/recombinant fowlpox virus (rFPV) boost regimen and monkeys vaccinated with a recombinant vaccinia virus prime/rFPV boost regimen developed comparable cellular immune responses that were greater in magnitude than those elicited by a homologous prime/boost with rMVA. Nevertheless, comparable magnitude recall cellular immune responses were observed in monkeys vaccinated with heterologous and homologous recombinant poxvirus following challenge with the CXCR4-tropic SHIV-89.6P. Consistent with this finding, comparable levels of containment of viral replication and CD4 super(+) T-lymphocyte preservation were seen in these groups of recombinant poxvirus-vaccinated monkeys. This study supports further exploration of combining recombinant vectors of the same family in prime/boost immunization strategies to optimize vaccine-elicited cellular immune responses. As the diversity of potential immunogens increases within certain classes of vectors, the possibility has arisen of employing heterologous prime/boost immunizations using diverse members of the same family of vectors. The present study was initiated to explore the use of divergent pox vectors in a prime/boost regimen to elicit high-frequency cellular immune responses to human immunodeficiency virus type 1 envelope and simian immunodeficiency virus gag in rhesus monkeys. We demonstrated that monkeys vaccinated with a recombinant modified vaccinia virus Ankara (rMVA) prime/recombinant fowlpox virus (rFPV) boost regimen and monkeys vaccinated with a recombinant vaccinia virus prime/rFPV boost regimen developed comparable cellular immune responses that were greater in magnitude than those elicited by a homologous prime/boost with rMVA. Nevertheless, comparable magnitude recall cellular immune responses were observed in monkeys vaccinated with heterologous and homologous recombinant poxvirus following challenge with the CXCR4-tropic SHIV-89.6P. Consistent with this finding, comparable levels of containment of viral replication and CD4 + T-lymphocyte preservation were seen in these groups of recombinant poxvirus-vaccinated monkeys. This study supports further exploration of combining recombinant vectors of the same family in prime/boost immunization strategies to optimize vaccine-elicited cellular immune responses. As the diversity of potential immunogens increases within certain classes of vectors, the possibility has arisen of employing heterologous prime/boost immunizations using diverse members of the same family of vectors. The present study was initiated to explore the use of divergent pox vectors in a prime/boost regimen to elicit high-frequency cellular immune responses to human immunodeficiency virus type 1 envelope and simian immunodeficiency virus gag in rhesus monkeys. We demonstrated that monkeys vaccinated with a recombinant modified vaccinia virus Ankara (rMVA) prime/recombinant fowlpox virus (rFPV) boost regimen and monkeys vaccinated with a recombinant vaccinia virus prime/rFPV boost regimen developed comparable cellular immune responses that were greater in magnitude than those elicited by a homologous prime/boost with rMVA. Nevertheless, comparable magnitude recall cellular immune responses were observed in monkeys vaccinated with heterologous and homologous recombinant poxvirus following challenge with the CXCR4-tropic SHIV-89.6P. Consistent with this finding, comparable levels of containment of viral replication and CD4(+) T-lymphocyte preservation were seen in these groups of recombinant poxvirus-vaccinated monkeys. This study supports further exploration of combining recombinant vectors of the same family in prime/boost immunization strategies to optimize vaccine-elicited cellular immune responses. |
Author | Phillip D. Markham Yue Sun Dennis Panicali Michael S. Wyand Jenny G. Parvani Alicia Gomez-Yafal Kelledy Manson David C. Montefiori Norman L. Letvin Valerie Philippon Sampa Santra Gail Mazzara |
AuthorAffiliation | Division of Viral Pathogenesis, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02115, 1 Therion Biologics, 76 Rogers Street, Cambridge, Massachusetts 02142, 2 Advanced Bioscience Laboratories, Inc., 5510 Nicholson Lane, Kensington, Maryland 20895, 3 Department of Surgery, Laboratory for AIDS Vaccine Research and Development, Duke University Medical Center, Durham, North Carolina 27710 4 |
AuthorAffiliation_xml | – name: Division of Viral Pathogenesis, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02115, 1 Therion Biologics, 76 Rogers Street, Cambridge, Massachusetts 02142, 2 Advanced Bioscience Laboratories, Inc., 5510 Nicholson Lane, Kensington, Maryland 20895, 3 Department of Surgery, Laboratory for AIDS Vaccine Research and Development, Duke University Medical Center, Durham, North Carolina 27710 4 |
Author_xml | – sequence: 1 givenname: Sampa surname: SANTRA fullname: SANTRA, Sampa organization: Division of Viral Pathogenesis, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02115, United States – sequence: 2 surname: YUE SUN fullname: YUE SUN organization: Division of Viral Pathogenesis, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02115, United States – sequence: 3 givenname: David C surname: MONTEFIORI fullname: MONTEFIORI, David C organization: Department of Surgery, Laboratory for AIDS Vaccine Research and Development, Duke University Medical Center, Durham, North Carolina 27770, United States – sequence: 4 givenname: Norman L surname: LETVIN fullname: LETVIN, Norman L organization: Division of Viral Pathogenesis, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02115, United States – sequence: 5 givenname: Jenny G surname: PARVANI fullname: PARVANI, Jenny G organization: Division of Viral Pathogenesis, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02115, United States – sequence: 6 givenname: Valerie surname: PHILIPPON fullname: PHILIPPON, Valerie organization: Therion Biologics, 76 Rogers Street, Cambridge, Massachusetts 02142, United States – sequence: 7 givenname: Michael S surname: WYAND fullname: WYAND, Michael S organization: Therion Biologics, 76 Rogers Street, Cambridge, Massachusetts 02142, United States – sequence: 8 givenname: Kelledy surname: MANSON fullname: MANSON, Kelledy organization: Therion Biologics, 76 Rogers Street, Cambridge, Massachusetts 02142, United States – sequence: 9 givenname: Alicia surname: GOMEZ-YAFAL fullname: GOMEZ-YAFAL, Alicia organization: Therion Biologics, 76 Rogers Street, Cambridge, Massachusetts 02142, United States – sequence: 10 givenname: Gail surname: MAZZARA fullname: MAZZARA, Gail organization: Therion Biologics, 76 Rogers Street, Cambridge, Massachusetts 02142, United States – sequence: 11 givenname: Dennis surname: PANICALI fullname: PANICALI, Dennis organization: Therion Biologics, 76 Rogers Street, Cambridge, Massachusetts 02142, United States – sequence: 12 givenname: Phillip D surname: MARKHAM fullname: MARKHAM, Phillip D organization: Advanced Bioscience Laboratories, Inc., 5510 Nicholson Lane, Kensington, Maryland 20895, United States |
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Cites_doi | 10.1073/pnas.0401954101 10.1097/01.qai.0000184857.39318.4f 10.1126/science.290.5491.486 10.1016/S0092-8674(01)00482-2 10.1089/aid.1991.7.991 10.1128/JVI.75.23.11603-11613.2001 10.4049/jimmunol.170.3.1416 10.1128/JVI.77.11.6305-6313.2003 10.1128/jvi.64.12.5948-5957.1990 10.1016/0076-6879(93)17089-N 10.1038/nature01470 10.1038/415331a 10.1126/science.1124226 10.1146/annurev.med.55.091902.104344 10.1126/science.1058915 10.1099/0022-1317-72-5-1031 10.4049/jimmunol.169.9.4778 10.1128/JVI.01458-06 10.1128/JVI.79.22.14161-14168.2005 10.1128/JVI.00558-06 10.1128/jvi.70.6.3741-3752.1996 10.1128/JVI.79.24.15547-15555.2005 10.1128/JVI.02392-06 10.1007/BF01641272 10.1073/pnas.0404620101 10.1073/pnas.93.21.11349 10.1007/978-1-4899-1382-1_2 10.4049/jimmunol.172.10.6290 |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Corresponding author. Mailing address: Division of Viral Pathogenesis, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, RE113, P.O. Box 15732, Boston, MA 02215. Phone: (617) 667-2766. Fax: (617) 667-8210. E-mail: nletvin@bidmc.harvard.edu |
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Mendeley... As the diversity of potential immunogens increases within certain classes of vectors, the possibility has arisen of employing heterologous prime/boost... ABSTRACT As the diversity of potential immunogens increases within certain classes of vectors, the possibility has arisen of employing heterologous prime/boost... |
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SubjectTerms | Animals Antibodies, Viral - blood Biological and medical sciences CD4 Lymphocyte Count Fowlpox virus Fundamental and applied biological sciences. Psychology Genetic Vectors - genetics Genetic Vectors - immunology Human immunodeficiency virus 1 Immunity, Cellular Immunization, Secondary - methods Macaca mulatta Microbiology Miscellaneous Poxviridae - genetics Poxviridae - immunology Poxvirus RNA, Viral - blood Simian immunodeficiency virus Vaccination - methods Vaccines and Antiviral Agents Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies Vaccinia virus Vaccinia virus - genetics Vaccinia virus - immunology Virology Virus Replication |
Title | Heterologous Prime/Boost Immunization of Rhesus Monkeys by Using Diverse Poxvirus Vectors |
URI | http://jvi.asm.org/content/81/16/8563.abstract https://www.ncbi.nlm.nih.gov/pubmed/17553898 https://search.proquest.com/docview/20331604 https://search.proquest.com/docview/70737037 https://pubmed.ncbi.nlm.nih.gov/PMC1951337 |
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